Rac family small GTPase 3

Summary
Gene Symbol
  • RAC3
Organism
Homo sapiens (human)
NCBI Gene
5881
HGNC
9803
PubChem
5881
Alliance of Genome Resources
Annotation
Keyword
  • 3D-structure
  • Cell membrane
  • Cell projection
  • Cytoskeleton
  • Disease variant
  • GTP-binding
  • Glycoprotein
  • Hydrolase
  • Intellectual disability
  • Isopeptide bond
  • Methylation
  • Prenylation
  • Reference proteome
  • Ubl conjugation
Proteins
Displaying 1 entry
UniProt Protein Name
P60763
  • p21-Rac3
Gene Ontology (GO)
GO Hierarchy
Displaying entries 1 - 5 of 21 in total
GO Term Evidence Code PMID
endoplasmic reticulum membrane
cytosol
cytoskeleton
plasma membrane
plasma membrane
GO Hierarchy
GO Hierarchy
OrthoDB (Group)
Group level
Eukaryota
Group Name
GTPase
Functional Category
  • T: Signal transduction mechanisms
  • U: Intracellular trafficking, secretion, and vesicular transport
Disease
The Human Phenotype Ontology
Displaying entries 1 - 10 of 26 in total
HPO ID HPO Term
HP:0000006 Autosomal dominant inheritance
HP:0000028 Cryptorchidism
HP:0000238 Hydrocephalus
HP:0000248 Brachycephaly
HP:0000289 Broad philtrum
HP:0000316 Hypertelorism
HP:0000343 Long philtrum
HP:0000347 Micrognathia
HP:0000431 Wide nasal bridge
HP:0000463 Anteverted nares
Displaying 1 entry
Disease ID Disease Name
OMIM:618577
  • neurodevelopmental disorder with structural brain anomalies and dysmorphic facies

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Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


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Last updated: December 8, 2025